RemedyRepack Lisinopril 10mg Tablets Recall: Foreign Metal Piece Hazard

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Contact the company & request your remedy

Recalling firmRemedyRepack Inc.625 Kolter Dr Ste 4 · Indiana, PA 15701-3571

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

RemedyRepack has recalled 10mg Lisinopril tablets that contain a metal piece in one tablet. This foreign material could cause injury if swallowed or ingested. The recall affects specific lot numbers from the repackaged product.

Why it’s dangerous

A small metal piece is embedded in one tablet of the recalled product. If swallowed, it could cause injury or internal damage. However, the hazard is contained to a single tablet and not the entire product.

Who’s affected

People who have the specific lot numbers of RemedyRepack's repackaged Lisinopril tablets (NDC# 70518-0468-00) are affected. Those with the metal piece in one tablet are at higher risk.

How to tell if you have this one

Check the blister card for the repackaged NDC# 70518-0468-00. Look for lot numbers J0636336-073022 or J0637605-080422. The product expires August 31, 2023.

Brand
RemedyRepack
Category
Drug

Based on the official FDA remedy

What to do — step by step

Check for Metal Piece
Inspect one tablet for a small metal piece. If found, stop using the product immediately.

✎ GovInfoNow

Questions people ask

Is there a remedy for this recall?

The official recall notice does not provide a remedy.

Which lot numbers are affected?

Lot numbers J0636336-073022 and J0637605-080422 are affected.

How can I tell if I have the recalled product?

Check the blister card for NDC# 70518-0468-00 and lot numbers J0636336-073022 or J0637605-080422.

Take action

Contact RemedyRepack

We’ve drafted a message you can send RemedyRepack to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall D-1538-2022 — RemedyRepack RemedyRepack

Hello,

I own a RemedyRepack that is covered by recall D-1538-2022 from RemedyRepack.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #D-1538-2022 (September 15, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1538-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

RemedyRepack Inc. recalls Lisinopril 10 mg tablets, 30-count Blister Card, Rx Only, MFG: Lupin Pharma, Baltimore, MD Repackaged by: RemedyRepack

Lower-risk recall